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Foundation Metal-Backed Patella

by Encore Orthopedics, Inc.

510(k) K932246

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK932246 Date22 Jul 1994DecidedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-1255-2010 FDA Unclassified (pre-2012) initiated 22 Feb 2010

    One lot of product was incorrectly manufactured. Pegs are larger than specification.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
JWH
Device Class
Class II
Regulation
21 CFR Part 888.3560
Advisory Committee
Orthopedic
FDA Decision
SN

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